1. Academic Validation
  2. An integrated microfluidic system for rapid screening of alpha-fetoprotein-specific aptamers

An integrated microfluidic system for rapid screening of alpha-fetoprotein-specific aptamers

  • Biosens Bioelectron. 2012 May 15;35(1):50-55. doi: 10.1016/j.bios.2012.02.024.
Chao-Jyun Huang 1 Hsin-I Lin 2 Shu-Chu Shiesh 3 Gwo-Bin Lee 4
Affiliations

Affiliations

  • 1 Department of Engineering Science, National Cheng Kung University, Tainan 70101, Taiwan.
  • 2 Department of Medical Laboratory Science and Biotechnology, National Cheng Kung University, Tainan 70101, Taiwan.
  • 3 Department of Medical Laboratory Science and Biotechnology, National Cheng Kung University, Tainan 70101, Taiwan. Electronic address: [email protected].
  • 4 Department of Power Mechanical Engineering, National Tsing Hua University, Hsinchu 30013, Taiwan. Electronic address: [email protected].
Abstract

The systematic evolution of ligands by exponential enrichment (SELEX) is a screening technique that involves the progressive selection of highly specific ligands via repeated rounds of partition and amplification from a large random pool of nucleic acid sequences. The products of this selection process are called Aptamers and are either short single-stranded deoxyribonucleic acid (ssDNA) or ribonucleic acid (RNA) molecules with a high binding affinity to a large variety of target analytes. However, SELEX is a lengthy, labor-intensive, iterative process requiring multiple rounds of extraction and polymerase chain reaction (PCR) amplification. In order to address these problems, this study presents a new integrated microfluidic system consisting of a magnetic bead-based microfluidic SELEX chip and a competitive assay chip to automate the aptamer screening process. More importantly, the selected ssDNA sequences were confirmed to have a high affinity and specificity to the target molecules, using the developed competitive assay chip. With this approach, an aptamer specific to alpha-fetoprotein (AFP), which is a biomarker for liver cancers, has been successfully selected. The screened aptamer was used as a recognition molecule for AFP and has a linear detection range from 12.5 to 800 ng/mL, which was suitable for rapid clinical applications.

Figures
Products